, Accounts of Chemical Research, vol.28, issue.7, pp.119-132, 1995.
, Journal of Organometallic Chemistry, vol.208, pp.419-427, 1981.
Chemistry3 : Introducing Inorganic, Organic and Physical Chemistry, vol.27, p.24, 2017. ,
Techniques de l'ingénieur Électrochimie, 2001. ,
, ) EEEEEEEEE, E. Nouvelles applications de la réaction de Passerini dans des réactions de type Friedel-Crafts et Tsuji-Trost., Ecole Polytechnique, vol.157, p.152, 2009.
DOI : 10.1021/ cr9409804, Chemical Society Reviews, vol.96, p.128, 1996. ,
, Tetrahedron Letters, vol.6, pp.4387-4388, 1965.
, J. Journal of the American Chemical Society, vol.95, p.128, 1973.
, Journal of the American Chemical Society, vol.86, p.129, 1964.
, Tetrahedron Letters, vol.11, p.129, 1970.
, The Journal of Organic Chemistry, vol.23, p.131, 1982.
, Tetrahedron Letters, vol.22, p.131, 1981.
, Tetrahedron Letters, vol.30, issue.00, p.133, 1989.
Chemtracts -Organic Chemistry, vol.12, p.133, 1999. ,
, Journal of the American Chemical Society, vol.97, issue.12, pp.81422-81429, 1975.
, Chemtracts -Organic Chemistry, vol.105, p.134, 1983.
, Journal of the American Chemical Society, vol.114, p.134, 1992.
, The Journal of Organic Chemistry, vol.63, p.134, 1998.
, Chemistry -A European Journal, vol.5, pp.615-621, 1999.
, , vol.92, pp.134-138, 2002.
, Gazz. Chim. Ital, vol.51, p.139, 1921.
, , vol.65, p.139, 2005.
, Angewandte Chemie International Edition in English, vol.23, p.139, 1958.
, Justus Liebigs Annalen der Chemie, vol.1867, p.139
, Justus Liebigs Annalen der Chemie, vol.1897, p.139
, Angewandte Chemie, vol.84, p.139, 1972.
, Angewandte Chemie, vol.71, p.139, 1959.
, , p.139, 2012.
, Multicomponent Reactions
, , p.139, 2005.
, Angewandte Chemie, vol.39, p.139, 2000.
, , p.141, 1971.
, Angewandte Chemie International Edition, vol.50, p.141, 2011.
, The Journal of Organic Chemistry, vol.77, p.141, 2012.
, , vol.44, p.142, 2005.
, Organic Letters, vol.8, p.142, 2006.
The Journal of Organic Chemistry, vol.72, p.142, 2007. ,
, Helvetica Chimica Acta, vol.66, p.142, 1983.
, Angewandte Chemie International Edition, vol.47, p.142, 2008.
, Journal of the American Chemical Society, vol.126, p.144, 2004.
, Tetrahedron Letters, vol.55, p.144, 2014.
, , p.145, 1901.
Advanced Synthesis & Catalysis, vol.358, p.145, 2016. ,
, Chemical Communications, vol.51, p.147, 2015.
, Chemical Communications, vol.52, p.147, 2016.
, European Journal of Organic Chemistry, vol.166, pp.146-148, 2017.
, , vol.26, p.150, 2015.
DOI : 10 . 1021 / om00029a052, European Journal of Organic Chemistry, vol.12, p.160, 1993. ,
, European Journal of Organic Chemistry, p.178, 2016.
, An apolar Varian VF-1ms (15 m x 0.25 mm internal diameter) capillary column was used. Three methods were used : 1. Injector: T inj 220 ? C; oven: ramp at 15 ? C min ?1 from 85 ? C to 230 ? C then holding at 230 ? C
, Injector: T inj 220 ? C; oven: isothermal at 230 ? C; detector: T det 250 ? C; H 2 flow: 1.0 mL min ?1 . This method has been used for the optimization of the reaction conditions
, Injector: T inj 220 ? C; oven: isothermal at 40 ? C for 3 min then ramp from 40 to 230 ? C at 15 ? C min ?1
, 5-dimethyphenylcarbamate)cellulose grafted on silica, length: 15 cm, = 4,6 mm, particle diameter: 5µm). solution of 79 (63.4 mg, 0.2 mmol, 1 equiv.) in DMF (in a 10 mL microwave suitable vial) were added successively Xantphos (13.9 mg, 24 µmol, 0.12 equiv.) and Pd(dba) 2 (11.5 mg, 20 µmol, 0.1 equiv.). The microwave tube was tightly closed and the reaction mixture was stirred at 80 ? C for 45 min. The solvent was removed under vacuum and the crude residue, Chiral HPLC analysis Chiral HPLC analysis was performed on a Agilent Technologies 1260 infinity apparatus, equiped with a Daicel chiralcel OD-H column (tris, vol.3
, H NMR attribution was performed on enriched fractions
, 300 MHz, Chloroform-d): ? / ppm 7.32 -7.11 (m, 10H, H Ar ), vol.6
, 6 Hz, 1H, C 3' -H), 6.30 (d, J = 16.0 Hz, 1H, C 3 -H), 5.51 (br d, vol.9
, 300 MHz, Chloroform-d): ? / ppm 7.32 -7.11 (m, 10H, H Ar ), vol.6
, 10.0 Hz, 1H, C 3' -H), 6.10 (d, J = 16.0 Hz, 1H, C 3 -H), 5.68 (br d, vol.9
, Both pairs (all peaks are split in two and reported here with an interpunct ·
, Chloroform-d): ? / ppm 173.6 · 172.2 (C 5 )
, C Ar ), 128.80 (C Ar ), 128.76 (C Ar ), 128.5 (C Ar ), 127.1 (C Ar ), 127.1 (C Ar ), C Ar ), vol.128, issue.2
, mg, 0.2 mmol, 1 equiv.) in DMF (in a 10 mL microwave suitable vial) were added successively Xantphos (13.9 mg, 24 µmol, 0.12 equiv.) and Pd(dba) 2 (11.5 mg, 20 µmol, 0.1 equiv.). The microwave tube was tightly closed and the reaction mixture was stirred at 80 ? C for 45 min, The solvent was removed under vacuum and the crude residue was purified by flash chromatography on silica gel (PE/AcOEt, vol.90
, H NMR attribution was performed on enriched fractions
, 300 MHz, Chloroform-d): ? / ppm 7.35 -7.20 (m, 10H, H Ar )
, 300 MHz, Chloroform-d): ? / ppm 7.35 -7.20 (m, 10H, H Ar ), vol.7
, 27 (d, J = 16.1 Hz, 1H, C 3 -H), 5.79 (dd, J = 15.3, 1.3 Hz, 1H, C 4, vol.6
, Both pairs (all peaks are split in two and reported here with an interpunct ·
, Chloroform-d): ? / ppm 172
, C 1 and C 1' ), 133.4 · 132.8 (C 2 ), 129.7 (C Ar ), vol.153